We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies, revised Privacy Policy and Terms of Service.
You are being directed to ZacksTrade, a division of LBMZ Securities and licensed broker-dealer. ZacksTrade and Zacks.com are separate companies. The web link between the two companies is not a solicitation or offer to invest in a particular security or type of security. ZacksTrade does not endorse or adopt any particular investment strategy, any analyst opinion/rating/report or any approach to evaluating individual securities.
If you wish to go to ZacksTrade, click OK. If you do not, click Cancel.
bluebird (BLUE) Resumes SCD & TDT Studies as FDA Lifts Hold
Read MoreHide Full Article
bluebird bio, Inc. (BLUE - Free Report) announced that the FDA lifted the clinical hold on the company’s clinical studies on gene therapies — LentiGlobin and betibeglogene autotemcel — for treating sickle cell disease (SCD) and transfusion-dependent β-thalassemia (TDT), respectively.
Following the development, the company will now be able to resume phase I/II HGB-206 and phase III HGB-210 studies on LentiGlobin (bb1111) for the treatment of adult and pediatric patients with SCD. It will also resume the phase III Northstar-2 (HGB-207) and Northstar-3 (HGB-212) studies on betibeglogene autotemcel (beti-cel) for treating adult, adolescent and pediatric patients with TDT.
Shares of bluebird were up 3.4% on Monday, following the announcement of the above-mentioned news. However, the stock has plunged 26.1% so far this year compared with the industry’s decrease of 4%.
Image Source: Zacks Investment Research
We remind investors that in February 2021, bluebird announced a temporary suspension of its phase I/II (HGB-206) and phase III (HGB-210) studies of LentiGlobin gene therapy for SCD (bb1111) due to a reported Suspected Unexpected Serious Adverse Reaction (SUSAR) of acute myeloid leukemia (AML).
As a result, the FDA placed a clinical hold on the HGB-206 and HGB-210 studies of LentiGlobin for SCD, and the HGB-207 and HGB-212 studies of beti-cel for β-thalassemia.
Subsequently, in March 2021, the company announced that it is very unlikely that the SUSAR of AML reported in its HGB-206 study of LentiGlobin for SCD was related to the BB305 lentiviral vector.
Notably, in 2019, the European Commission granted conditional marketing authorization for beti-cel (in patients aged 12 years or older, with transfusion-dependent β-thalassemia (TDT), who do not have a β0/β0 genotype and for whom hematopoietic stem cell (HSC) transplantation is appropriate but a human leukocyte antigen (HLA)-matched related HSC donor is not available. It is marketed as Zynteglo.
bluebird remains on track to complete its rolling biologics license application submission to the FDA in mid-2021 for beti-cel.
Repligen’s earnings estimates have been revised 15.7% upward for 2021 and 14.7% upward for 2022 over the past 60 days.
Kamada’s earnings estimates have been revised 21.4% upward for 2021 and 18.1% upward for 2022 over the past 60 days.
Bio-Techne’s earnings estimates have been revised 8.8% upward for 2021 and 9.1% upward for 2022 over the past 60 days. The stock has gained 32.1% year to date.
More Stock News: This Is Bigger than the iPhone!
It could become the mother of all technological revolutions. Apple sold a mere 1 billion iPhones in 10 years but a new breakthrough is expected to generate more than 77 billion devices by 2025, creating a $1.3 trillion market.
Zacks has just released a Special Report that spotlights this fast-emerging phenomenon and 4 tickers for taking advantage of it. If you don't buy now, you may kick yourself in 2022.
Image: Bigstock
bluebird (BLUE) Resumes SCD & TDT Studies as FDA Lifts Hold
bluebird bio, Inc. (BLUE - Free Report) announced that the FDA lifted the clinical hold on the company’s clinical studies on gene therapies — LentiGlobin and betibeglogene autotemcel — for treating sickle cell disease (SCD) and transfusion-dependent β-thalassemia (TDT), respectively.
Following the development, the company will now be able to resume phase I/II HGB-206 and phase III HGB-210 studies on LentiGlobin (bb1111) for the treatment of adult and pediatric patients with SCD. It will also resume the phase III Northstar-2 (HGB-207) and Northstar-3 (HGB-212) studies on betibeglogene autotemcel (beti-cel) for treating adult, adolescent and pediatric patients with TDT.
Shares of bluebird were up 3.4% on Monday, following the announcement of the above-mentioned news. However, the stock has plunged 26.1% so far this year compared with the industry’s decrease of 4%.
Image Source: Zacks Investment Research
We remind investors that in February 2021, bluebird announced a temporary suspension of its phase I/II (HGB-206) and phase III (HGB-210) studies of LentiGlobin gene therapy for SCD (bb1111) due to a reported Suspected Unexpected Serious Adverse Reaction (SUSAR) of acute myeloid leukemia (AML).
As a result, the FDA placed a clinical hold on the HGB-206 and HGB-210 studies of LentiGlobin for SCD, and the HGB-207 and HGB-212 studies of beti-cel for β-thalassemia.
Subsequently, in March 2021, the company announced that it is very unlikely that the SUSAR of AML reported in its HGB-206 study of LentiGlobin for SCD was related to the BB305 lentiviral vector.
Notably, in 2019, the European Commission granted conditional marketing authorization for beti-cel (in patients aged 12 years or older, with transfusion-dependent β-thalassemia (TDT), who do not have a β0/β0 genotype and for whom hematopoietic stem cell (HSC) transplantation is appropriate but a human leukocyte antigen (HLA)-matched related HSC donor is not available. It is marketed as Zynteglo.
bluebird remains on track to complete its rolling biologics license application submission to the FDA in mid-2021 for beti-cel.
Zacks Rank & Stocks to Consider
bluebird currently carries a Zacks Rank #3 (Hold). Some better-ranked stocks in the biotech sector are Repligen Corporation (RGEN - Free Report) , Kamada Ltd. and Bio-Techne Corporation (TECH - Free Report) , all carrying a Zacks Rank #2 (Buy) at present. You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.
Repligen’s earnings estimates have been revised 15.7% upward for 2021 and 14.7% upward for 2022 over the past 60 days.
Kamada’s earnings estimates have been revised 21.4% upward for 2021 and 18.1% upward for 2022 over the past 60 days.
Bio-Techne’s earnings estimates have been revised 8.8% upward for 2021 and 9.1% upward for 2022 over the past 60 days. The stock has gained 32.1% year to date.
More Stock News: This Is Bigger than the iPhone!
It could become the mother of all technological revolutions. Apple sold a mere 1 billion iPhones in 10 years but a new breakthrough is expected to generate more than 77 billion devices by 2025, creating a $1.3 trillion market.
Zacks has just released a Special Report that spotlights this fast-emerging phenomenon and 4 tickers for taking advantage of it. If you don't buy now, you may kick yourself in 2022.
Click here for the 4 trades >>